Association and linkage between an insulin-like growth factor-1 gene polymorphism and fat free mass in the HERITAGE Family Study

Citation
G. Sun et al., Association and linkage between an insulin-like growth factor-1 gene polymorphism and fat free mass in the HERITAGE Family Study, INT J OBES, 23(9), 1999, pp. 929-935
Citations number
37
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
INTERNATIONAL JOURNAL OF OBESITY
ISSN journal
03070565 → ACNP
Volume
23
Issue
9
Year of publication
1999
Pages
929 - 935
Database
ISI
SICI code
0307-0565(199909)23:9<929:AALBAI>2.0.ZU;2-C
Abstract
OBJECTIVE: To investigate the relationship between a DNA microsatellite mar ker in the insulin-like growth factor-1 (IGF-1) gene and body composition p henotypes before and following exposure to 20 weeks of aerobic exercise tra ining in the HERITAGE Family Study. DESIGN: A controlled intervention study: fat mass (FM), percentage body fat (%FAT), fat free mass (FFM), body mass index (BMI) and abdominal visceral fat (AVF) at baseline (8) and in response to training (Delta = post minus p re-training value) were measured, Association and sib-pair linkage studies were undertaken. SUBJECTS: A maximum of 502 Caucasian individuals (99 families; 190 parents and 312 adult offspring). MEASUREMENTS: The polymorphism was typed by polymerase chain reaction and D NA sequencer. The body composition phenotypes were determined from the unde rwater weighing method, and AVF was assessed by computerized tomography sca n. RESULTS: 11 alleles were found: the lengths ranged from 189 to 209 base pai rs (bp), and the frequency of the most common allele, 189 bp, reached 0.71. In association studies, significant differences for B-FM, B-FFM and B-%FAT among the three genotypes (189 bp homozygotes, heterozygotes and non-carri ers) were detected. The B-FM for 189 bp homozygotes was 19.7 +/- 0.6 kg, bu t 21.6 +/- 0.7 and 21.3 +/- 1.5 kg for the 189 bp heterozygotes and the non -189 bp carriers respectively (P = 0.03 after adjustment for age, sex and g eneration), Differences among the three genotypes were also observed for B- %FAT (25.9 +/- 0.5 versus 27.4 +/- 0.6 and 26.6 +/- 1.2 kg; P < 0.05) and B -FFM (53.7 +/- 0.4 versus 54.9 +/- 0.5 kg and 54.4 +/- 1.0 kg; P < 0.05). N o significant difference for B-AVF was found among the three genotypes. Fol lowing 20 weeks of endurance exercise, the 189 bp homozygotes gained only a bout half the amount of FFM compared with the other two IGF-1 genotypes (0. 3 +/- 0.1 vs 0.7 +/- 0.1 and 0.5 +/- 0.2 kg; P = 0.005). A strong linkage w as observed between the IGF-1 marker and the changes in FFM (308 pairs of f ull sibs, P = 0.0002) but only a suggestive linkage with B-AVF (352 pairs o f full sibs, P < 0.02). CONCLUSION: Associations were detected between the IGF-1 gene marker and FM , %FAT and FFM at baseline, acid a strong association with the changes in F FM in response to training, Moreover, the IGF-1 gene marker was found to be strongly linked to the changes in FFM in response to 20 weeks of endurance exercise and weakly linked to abdominal visceral fat in the sedentary stat e.